2oh4
From Proteopedia
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Crystal structure of Vegfr2 with a benzimidazole-urea inhibitor
Contents |
Overview
We herein disclose a novel chemical series of benzimidazole-ureas as, inhibitors of VEGFR-2 and TIE-2 kinase receptors, both of which are, implicated in angiogenesis. Structure-activity relationship (SAR) studies, elucidated a critical role for the N1 nitrogen of both the benzimidazole, (segment E) and urea (segment B) moieties. The SAR results were also, supported by the X-ray crystallographic elucidation of the role of the N1, nitrogen and the urea moiety when the benzimidazole-urea compounds were, bound to the VEGFR-2 enzyme. The left side phenyl ring (segment A), occupies the backpocket where a 3-hydrophobic substituent was favored for, TIE-2 activity.
Disease
Known disease associated with this structure: Hemangioma, capillary infantile, somatic OMIM:[191306]
About this Structure
2OH4 is a Single protein structure of sequence from Homo sapiens with SO4 and GIG as ligands. Active as Receptor protein-tyrosine kinase, with EC number 2.7.10.1 Full crystallographic information is available from OCA.
Reference
Discovery of Novel Benzimidazoles as Potent Inhibitors of TIE-2 and VEGFR-2 Tyrosine Kinase Receptors., Hasegawa M, Nishigaki N, Washio Y, Kano K, Harris PA, Sato H, Mori I, West RI, Shibahara M, Toyoda H, Wang L, Nolte RT, Veal JM, Cheung M, J Med Chem. 2007 Sep 6;50(18):4453-70. Epub 2007 Aug 4. PMID:17676829
Page seeded by OCA on Mon Nov 12 23:10:49 2007
Categories: Homo sapiens | Receptor protein-tyrosine kinase | Single protein | Nolte, R.T. | Wang, L. | GIG | SO4 | Transferase | Vascular endothelial growth factor receptor 2 tyrosine-protein kinase 3d-structure vegfr2 angiogenesis atp-binding phosphorylation ec 2.7.1.112 vegfr-2 kinase insert domain receptor protein-tyrosine kinase receptor flk-1
